Assemblies including an oxygen-sensing assembly

ABSTRACT

An oxygen-sensing assembly for attachment to a urinary catheter may include a housing having a flow pathway extending between an inlet end and an outlet end thereof, an oxygen sensor in operable communication with the flow pathway of the housing, the oxygen sensor configured to detect oxygen levels of a fluid flowing through the flow pathway, a flowrate sensor configured to detect a flowrate of the fluid flowing through the flow pathway, and a temperature sensor configured to detect a temperature of the fluid flowing through the flow pathway.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No.16/121,372, filed Sep. 4, 2018, which claims the benefit under 35 U.S.C.§ 119(e) of U.S. Provisional Patent Application Ser. No. 62/555,161,filed Sep. 7, 2017, the disclosure of each of which is herebyincorporated herein in its entirety by this reference.

FIELD

Embodiments of the present disclosure relate generally to urinarycatheter assemblies and oxygen-sensing assemblies. Additionally,embodiments of the present disclosure relate generally to measuringoxygen tension within fluids and determining risk of acute kidney injury(e.g., urinary hypoxia) in patients.

BACKGROUND

Acute kidney injury (hereinafter “AKI”) is an unfortunately commoncomplication of cardiac surgery that occurs in up to 40% of patients andresults in increased mortality, prolonged intensive care unit stays, andprolonged hospital stays. Patients with AKI after cardiac surgery havebeen shown to have 39 times the mortality rate as patients without AKI.AKI has also been associated with increased morbidity and a largernumber of patients requiring discharge to an extended care facility.

Conventionally, diagnosing AKI has been based on either a sustaineddecrease in urine output or a rise in serum creatinine. A majorlimitation of utilizing serum creatinine levels and urine output asmarkers of kidney function and renal injury is that there is asignificant time lag between an actual injury and diagnosis. Forinstance, it often takes 24 to 36 hours after renal injury for serumcreatinine levels to increase. As a result, diagnosis of AKI via theforegoing method is delayed by at least 24 to 36 hours. Additionally,perioperative urine output is affected by volume status, anestheticdrugs, and the use of diuretics, and AKI is typically not diagnoseduntil oliguria has occurred for at least 6 to 12 hours. Accordingly, theinherent time lags in measuring serum creatinine and an uncertainties inmeasuring urinary output render the measurements insensitive to acutechanges in renal function and relatively useless in the prevention ofAKI during and after cardiac surgery.

More recently, several early biomarkers have been developed to identifypatients whom are at risk for developing AKI. Several of thesebiomarkers have been used for the early prediction of AKI in cardiacsurgery patients. However, even these biomarkers still do not indicateAKI until at least 3 to 4 hours (and in some cases, 24 hours) afterrenal injury.

Accordingly, one of the major limitations in the efforts to reduce theincidence of AKI in cardiac surgery is the lack of a real-time monitorof renal perfusion. As mentioned above, urine output is well known to bea poor indicator of renal perfusion. While urinary flowrate may belinearly related to blood pressure while on a cardiopulmonary bypass(“CPB”), this is likely related to a phenomenon called “pressurediuresis” and is unlikely to be a reflection of improved renalperfusion. Renal blood flow can be measured by cannulating the renalvein through a central venous catheter placed in the femoral vein. This,however, is a highly invasive technique and is not utilized routinely.

As a result of the lack of real-time monitoring of the kidneys duringcardiac surgery, anesthesiologists are often left to make educatedguesses as to which blood pressures and cardiac outputs are adequate forrenal perfusion based on the patient's baseline blood pressure andkidney function. In a patient with a long history of hypertension and/orchronic kidney disease the anesthesiologist's goal is often to try tomaintain a higher mean arterial pressure (MAP) both on and off CPB thannormal in order to improve renal perfusion.

Medullary hypoxia may be a consequence of decreased oxygen delivery orincreased oxygen consumption and is a major determinant of AKI andchronic kidney disease. The relatively hypoxic environment of the renalmedulla and its role in renal injury suggests that global measures ofsystemic venous oxygenation through a central venous catheter or evenrenal venous oxygenation through an invasive renal vein catheter may bepoor monitors of adequate renal perfusion. Due to the physical proximityof the vasa recta in the renal medulla with the urinary collectingducts, medullary oxygen tension is more closely related to urinaryoxygen tension than renal venous oxygenation.

Accordingly, these and other disadvantages exist with respect toconventional methods and systems for diagnosing AKI in cardiac surgerypatients.

BRIEF SUMMARY

Some embodiments of the present disclosure include a catheter assembly,including a urinary catheter, an oxygen-sensing assembly, and a controlsystem. The urinary catheter may include a lumen extending between aninlet end and an outlet end thereof. The oxygen-sensing assembly may bein fluid communication with the urinary catheter. The oxygen-sensingassembly may include a housing having a flow pathway extending betweenan inlet end and an outlet end thereof, wherein the inlet end of thehousing is attachable to the outlet end of the urinary catheter, anoxygen sensor in operable communication with the flow pathway of thehousing, the oxygen sensor configured to detect oxygen levels of a fluidflowing through the flow pathway, a flowrate sensor disposed between theoxygen sensor and the inlet end of the housing and configured to detecta flowrate of the fluid flowing through the flow pathway, and atemperature sensor disposed downstream of the oxygen sensor andconfigured to detect a temperature of the fluid flowing through the flowpathway. The control system may be operably coupled to the oxygensensor, the flowrate sensor, and the temperature sensor. The controlsystem may include at least one processor and at least onenon-transitory computer-readable storage medium storing instructionsthereon that, when executed by the at least one processor, cause thecontrol system to: receive a detected and/or calculated oxygen levels, adetected and/or calculated flowrate, and a detected temperature of thefluid flowing through the flow pathway and based at least partially onone or more of the detected oxygen levels and the detected temperature,determine a measurement of an oxygen tension of the fluid flowingthrough the flow pathway of the housing.

One or more embodiments of the present disclosure includes anoxygen-sensing assembly for attachment to a urinary catheter. Theoxygen-sensing assembly may include a housing having a flow pathwayextending between an inlet end and an outlet end thereof and an oxygensensor in operable communication with the flow pathway of the housing,the oxygen sensor configured to detect oxygen levels of a fluid in orflowing through the flow pathway.

Some embodiments of the present disclosure include a method thatincludes attaching an oxygen-sensing assembly to a urinary catheter;disposing the urinary catheter within a bladder of a subject; detectingoxygen levels of a fluid flowing through the urinary catheter andthrough a flow pathway of a housing of the oxygen-sensing assembly withan oxygen sensor; detecting a flowrate of the fluid flowing through theflow pathway with a flowrate sensor; detecting a temperature of thefluid flowing through the flow pathway with a temperature sensor; andbased at least partially on one or more of the detected and/orcalculated oxygen levels and the detected and/or calculated temperatureof the fluid, determining a measurement of an oxygen tension of thefluid flowing through the flow pathway.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic representation of a catheter assembly having anoxygen-sensing assembly according to one or more embodiments of thepresent disclosure;

FIG. 2 is a schematic representation of an oxygen sensor according toone or more embodiments of the present disclosure;

FIG. 3 is a flow diagram illustrating a method flow that a catheterassembly may utilize to determine oxygen tension within urine of apatient;

FIG. 4 is a schematic representation of a catheter assembly having anoxygen-sensing assembly having a check valve configuration according toadditional embodiments of the present disclosure; and

FIG. 5 is a schematic representation of a catheter assembly having anoxygen-sensing assembly having an additional check valve configurationaccording to additional embodiments of the present disclosure.

DETAILED DESCRIPTION

The illustrations presented herein are not actual views of anyparticular catheter assembly, but are merely idealized representationsemployed to describe example embodiments of the present disclosure. Thefollowing description provides specific details of embodiments of thepresent disclosure in order to provide a thorough description thereof.However, a person of ordinary skill in the art will understand that theembodiments of the disclosure may be practiced without employing manysuch specific details. Indeed, the embodiments of the disclosure may bepracticed in conjunction with conventional techniques employed in theindustry. In addition, the description provided below does not includeall elements to form a complete structure or assembly. Only thoseprocess acts and structures necessary to understand the embodiments ofthe disclosure are described in detail below. Additional conventionalacts and structures may be used. Also note, any drawings accompanyingthe application are for illustrative purposes only, and are thus notdrawn to scale. Additionally, elements common between figures may havecorresponding numerical designations.

As used herein, the terms “comprising,” “including,” and grammaticalequivalents thereof are inclusive or open-ended terms that do notexclude additional, un-recited elements or method steps, but alsoinclude the more restrictive terms “consisting of,” “consistingessentially of,” and grammatical equivalents thereof.

As used herein, the term “may” with respect to a material, structure,feature, or method act indicates that such is contemplated for use inimplementation of an embodiment of the disclosure, and such term is usedin preference to the more restrictive term “is” so as to avoid anyimplication that other compatible materials, structures, features, andmethods usable in combination therewith should or must be excluded.

As used herein, the term “configured” refers to a size, shape, materialcomposition, and arrangement of one or more of at least one structureand at least one apparatus facilitating operation of one or more of thestructure and the apparatus in a predetermined way.

As used herein, the singular forms following “a,” “an,” and “the” areintended to include the plural forms as well, unless the context clearlyindicates otherwise.

As used herein, the term “and/or” includes any and all combinations ofone or more of the associated listed items.

As used herein, spatially relative terms, such as “below,” “lower,”“bottom,” “above,” “upper,” “top,” and the like, may be used for ease ofdescription to describe one element's or feature's relationship toanother element(s) or feature(s) as illustrated in the figures. Unlessotherwise specified, the spatially relative terms are intended toencompass different orientations of the materials in addition to theorientation depicted in the figures. For example, the spatially relativeterms may refer to a catheter assembly when the catheter is placed in apatient.

As used herein, the term “substantially” in reference to a givenparameter, property, or condition means and includes to a degree thatone of ordinary skill in the art would understand that the givenparameter, property, or condition is met with a degree of variance, suchas within acceptable manufacturing tolerances. By way of example,depending on the particular parameter, property, or condition that issubstantially met, the parameter, property, or condition may be at least90.0% met, at least 95.0% met, at least 99.0% met, or even at least99.9% met.

FIG. 1 shows a catheter assembly 100 according to one or moreembodiments of the present disclosure. The catheter assembly 100 mayinclude a urinary catheter 102, an oxygen-sensing assembly 104 in fluidcommunication with the urinary catheter 102, and a control system 106operably coupled to the oxygen-sensing assembly 104.

The urinary catheter 102 may include an inlet end 108, an outlet end110, and a lumen 112 extending between the inlet end 108 and the outletend 110. In some embodiments, the urinary catheter 102 may include aFoley catheter. For instance, the urinary catheter 102 may include aflexible tube that may be passed (e.g., inserted) through the urethra ofa patient and into the bladder of the patient in order to drain urine.Furthermore, in some embodiments, the urinary catheter 102 and theoxygen-sensing assembly 104 may form a single integral unit. As will beappreciated by one of ordinary skill in the art, the urinary catheter102 may further include a balloon 114 proximate the inlet end 108 thatcan be inflated with sterile water once the urinary catheter 102 hasbeen placed and when the balloon 114 lies within the bladder of thepatient. The balloon 114 may prevent the urinary catheter 102 fromslipping out of the bladder of the patient. Additionally, the urinarycatheter 102 may include a balloon port 116 for inflating the balloon114. As will be described in greater detail below, in some embodimentsof the present disclosure, the urinary catheter 102 may include one ormore additional lumens that may provide an access port for one or moreoxygen sensors of the present disclosure.

As noted above, the oxygen-sensing assembly 104 may be in fluidcommunication with the urinary catheter 102 and may include a housing118, an oxygen sensor 120, a flowrate sensor 122, and a temperaturesensor 124. The housing 118 may include an inlet end 126 and an outletend 128 and may define a flow pathway 130 between the inlet end 126 andthe outlet end 128. The inlet end 126 of the housing 118 may beattachable to the outlet end 110 of the urinary catheter 102 via anyconnection methods known in the art. The oxygen sensor 120, the flowratesensor 122, and the temperature sensor 124 may be disposed along theflow pathway 130 in series. Furthermore, although a specific componentorder is illustrated in FIG. 1, the disclosure is not so limited, andthe oxygen sensor 120, the flowrate sensor 122, and the temperaturesensor 124 may be positioned in any order. Moreover, in one or moreembodiments, one or more of the oxygen sensor 120, the flowrate sensor122, and the temperature sensor 124 may be positioned in parallel withanother of the oxygen sensor 120, the flowrate sensor 122, and thetemperature sensor 124. Additionally, in some embodiments, one or moreof the oxygen sensor 120, the flowrate sensor 122, and the temperaturesensor 124 may be combined into a single sensor.

In some embodiments, the flowrate sensor 122 may include a liquid flowmeter. For instance, the flowrate sensor 122 may detect and determine aflowrate of a fluid (e.g., urine) through the flow pathway 130 of theoxygen-sensing assembly 104. Many such flowrate sensors are known in theart, and the flowrate sensor 122 may comprise any of the flow sensorsknown in the art. Furthermore, the flowrate sensor 122 may be operablycoupled to the control system 106 and may provide data related to aflowrate of the fluid through the flow pathway 130 to the control system106. For instance, as is described in greater detail below, the controlsystem 106 may utilize data from the flowrate sensor 122 to assist inqualifying an oxygen tension (PuO2) measurement within urine through theflow pathway 130 (i.e., determine whether the oxygen tension (PuO2)measurement is relevant to bladder and/or kidney oxygen tensions), todetermine a risk of acute kidney injury (e.g., urinary hypoxia) of apatient. Additionally, the control system 106 may utilize data from theflowrate sensor 122 to determine (e.g., back calculate) an oxygentension (PuO2) measurement of the bladder and/or kidney of the patient.For instance, the control system 106 utilizes the flowrate sensor 122 todetermine how long the urine has been out of the bladder and/or kidneysof the patient prior to being measured with the oxygen sensor 120 and/ortemperature sensor 124. In one or more embodiments, the flowrate sensor122 may be positioned downstream of the oxygen sensor 120 along the flowpathway 130 of the oxygen-sensing assembly 104. Furthermore, in someinstance, the flowrate sensor 122 may heat urine passing throughflowrate sensor 122. As a result, disposing the flowrate sensor 122downstream of the oxygen sensor 120 may be advantageous in order toavoid having the oxygen sensor 120 measuring heated urine. Furthermore,having oxygen sensing upstream, or closer to an outlet end 110 of theurinary catheter 102 may be advantageous because oxygen sensing upstreamshortens a path that the urine must travel from a kidney to a sensor(e.g., the oxygen sensor 120). As a result, the oxygen sensing methodsdescribed herein shorten a lag between the sensor's readings and what isactually occurring within the kidney. In other embodiments, the flowratesensor 122 may be positioned upstream of the oxygen sensor 120 along theflow pathway 130 of the oxygen-sensing assembly 104.

In one or more embodiments, the oxygen sensor 120 may be at leastpartially disposed within the flow pathway 130 of the oxygen-sensingassembly 104. Furthermore, the oxygen sensor 120 may detect oxygenlevels within urine passing through (i.e., flowing through) the flowpathway 130 of the oxygen-sensing assembly 104. In some embodiments, theoxygen sensor 120 may include a fiber optic sensor. For instance, theoxygen sensor 120 may include an optical fiber 132 and a sensing portion134. As a non-limiting example, the oxygen sensor 120 may include aFiber Bragg grating sensor. The optical fiber 132 may be operablycoupled to an optical module 136 of the control system 106 and mayextend at least partially into the housing 118 of the oxygen-sensingassembly 104. The sensing portion 134 may be disposed at least partiallywithin the flow pathway 130 of the oxygen-sensing assembly 104 and maybe exposed to the fluid (e.g., urine) flowing through the flow pathway130 of the oxygen-sensing assembly 104.

In some embodiments, the sensing portion 134 of the oxygen sensor 120may be secured to a distal end of the optical fiber 132. In otherembodiments, the sensing portion 134 of the oxygen sensor 120 may beseparated from the optical fiber 132 (e.g., may be separate and distinctfrom the optical fiber 132). In embodiments where the sensing portion134 of the oxygen sensor 120 is separate and distinct from the opticalfiber 132, the oxygen sensor 120 may include a barrier member 138 (e.g.,a polymer wall) between the sensing portion 134 and the optical fiber132. The barrier member 138 may prevent the optical fiber 132 fromcoming into contact with (e.g., being contaminated by) the fluid (e.g.,urine) flowing through the flow pathway 130 of the housing 118 of theoxygen-sensing assembly 104. As a result, use of the barrier member 138enables the optical fiber 132 to be reusable with other oxygen-sensingassemblies. In further embodiments, the oxygen sensor 120 may notinclude an optical fiber 132 and the oxygen-sensing assembly 104 mayemit light from and may detect light at the sensing portion 134. Thestructure of the oxygen sensor 120 is described in greater detail inbelow in regard to FIG. 2.

As will be appreciated by one of ordinary skill in the art, inoperation, the optical fiber 132 of the oxygen sensor 120 may transmitlight (e.g., excitation light) from the optical module 136 of thecontrol system 106 (e.g., emitted and/or generated by the optical module136) through a distal end of the optical fiber 132 and at (i.e., toward)the sensing portion 134 of the oxygen sensor 120. Additionally, theoptical fiber 132 may transmit light (e.g., return light) emitted and/orreflected by (e.g., light originated at) the sensing portion 134 of theoxygen sensor 120 through the distal end of the optical fiber 132 andmay transmit the return light back to the optical module 136 and controlsystem 106 for analysis.

In some embodiments, the optical fiber 132 may include a core and acladding, which is known in the art. For example, the optical fiber 132may include a single mode fiber, a multi-mode fiber, or special-purposefiber (e.g., an optical fiber constructed with a non-cylindrical coreand/or cladding layer). Furthermore, the optical fiber 132 may includeone or more of a step-index multi-mode fiber, a graded-index multimodefiber, a loose-tube cable, or a tight-buffered cable. In one or moreembodiments, the core of the optical fiber 132 may include one or moreof silica, fluorozirconate glass, fluoroaluminate glass, chalcogenideglass, fluoride glass, phosphate glass, poly(methyl methacrylate), orpolystyrene. Additionally, the cladding of the optical fiber 132 mayinclude fluorinated polymers. For example, the optical fiber 132 mayinclude any optical fiber known in the art.

In some embodiments, the sensing portion 134 may include adye-impregnated polymer or silica impregnated with fluorescent dyes,which dyes are excitable at selected wavelengths of light. In one ormore embodiments, the dyes may be oxygen sensitive and may beimmobilized (e.g., impregnated) within a polymer matrix. For example,the dyes may be sensitive to oxygen such that the oxygen quenches afluorescence response of the dyes. Additionally, in some embodiments,the polymer or silica may be applied to a carrier material such as afoil and may be separate from the optical fiber 132. Moreover, as notedabove, in some embodiments, the polymer may be coated directly onto theoptical fiber 132. As a non-limiting example, the sensing portion 134may include any fluorescence quenching oxygen sensor known in the art.

In some embodiments, the dye of the sensing portion 134 may include oneor more of a platinum(II) based dye, a palladium(II) based dye, aruthenium(II) based dye, or a hemoglobin based dye. For example, the dyemay include platinum octaethylporphyrin. Furthermore, the sensingportion 134 may include any other dyes known in the art.

In operation, the optical fiber 132 may transmit excitation light fromthe optical module 136 of the control system 106 to the sensing portion134 of the oxygen sensor 120, which is exposed to urine and any oxygenmolecules within the urine. Additionally, simultaneously, the opticalfiber 132 may transmit a fluorescence response (i.e., emission of lightby a substance not resulting from heat and a form of cold-bodyradiation) of the sensing portion 134 (e.g., return light) to theoptical module 136 of the control system 106 for analysis. Furthermore,depending on the amount of oxygen molecules that are (e.g., an oxygenconcentration) present in the urine flowing through the flow pathway 130of the oxygen-sensing assembly 104, the luminescence response (e.g., thereturn light) of the sensing portion 134 may vary. For instance, thefluorescence response may be quenched by the presence of the oxygenmolecules. In other words, the fluorescence response of the sensingportion 134 may decrease as a concentration of oxygen increases withinthe fluid. In additional embodiments, the luminescence response mayinclude amplitudes of the fluorescent response.

As a non-limiting example, in some embodiments, the optical module 136of the control system 106 may provide (e.g., generate) a sinusoidallymodulated excitation light (e.g., an excitation beam having a wavelengthof about 432 nm). Furthermore, shining the foregoing excitation light onthe sensing portion 134 of the oxygen sensor 120 may result in aphase-shifted sinusoidally modulated return light (e.g., a return beamhaving a wavelength of about 760 nm). As is discussed in greater detailin regard to FIG. 3, upon receiving the return light through the opticalmodule 136, the control system 106 may measure a phase shift of thephase-shifted sinusoidally modulated return light relative to thesinusoidally modulated excitation light. Furthermore, the control system106 may determine oxygen levels of the fluid (e.g., concentrations ofoxygen within the fluid) based on the phase shift and based on theStern-Vollmer-Theory. For instance, control system 106 may determineoxygen levels of the fluid based on the phase shift of the return lightutilizing the following Stern-Vollmer Equation:

$\frac{F_{0}}{F} = {1 + {K_{SV}\lbrack Q\rbrack}}$

where F₀ and F represent the fluorescence intensities observed in theabsence (e.g., sinusoidally modulated excitation light) and in thepresence (e.g., phase-shifted sinusoidally modulated return light) of aquencher. [Q] represents a quencher concentration (e.g., oxygenconcentration) and K_(SV) represents the Stern-Vollmer quenchingconstant. The operation of the oxygen sensor 120 is described in greaterdetail in regard to FIGS. 2 and 3.

Referring still to FIG. 1, in some embodiments, the oxygen sensor 120may include an electrochemical oxygen sensor. For instance, the oxygensensor 120 may include a polarographic sensor. As a non-limitingexample, the oxygen sensor 120 may include a Clark electrode, whichmeasures ambient oxygen concentration within a liquid using a catalyticplatinum surface according to the following net reaction:

O₂+4e ⁻+4H⁺→2H₂O

In additional embodiments, the oxygen sensor 120 may include a pulsedpolarographic sensor. In further embodiments, the oxygen sensor 120 mayinclude a galvanic sensor (e.g., an electro-galvanic fuel cell), as isknown in the art.

In additional embodiments, the oxygen sensor 120 may include acolorimetric oxygen sensor. For example, the oxygen sensor 120 mayutilize the Indigo Carmine Method (as known in the art) to determineoxygen levels within the fluid flowing through the flow pathway 130 ofthe housing 118 of the oxygen-sensing assembly 104. In furtherembodiments, the oxygen sensor 120 may utilize the Rhodazine Method (asknown in the art) to determine oxygen levels within the fluid.

Regardless of the type of oxygen sensor utilized, the oxygen sensor 120,in conjunction with the control system 106, may be used to detect anddetermine a concentration of oxygen (e.g., an amount of oxygen pervolume of fluid) within the fluid (e.g., urine) flowing through the flowpathway 130 of the oxygen-sensing assembly 104. For instance, utilizingthe oxygen sensor 120, the control system 106 may determine a partialpressure of oxygen, a dissolved oxygen concentration, a head spaceoxygen gas concentration, a dissolved oxygen reading, etc., of thefluid. Furthermore, the control system 106 may determine oxygen levelswithin the fluid in real-time.

Referring still to FIG. 1, in some embodiments, the temperature sensor124 may be downstream of the oxygen sensor 120 along the flow pathway130 of the oxygen-sensing assembly 104. In other embodiments, thetemperature sensor 124 may be positioned upstream of the oxygen sensor120. In some embodiments, having the temperature sensor 124 downstreamof the oxygen sensor 120 may be advantageous as it may enabledetermining that a temperature of the urine passing by the oxygen sensor120 is within a range of a body temperature of the patient and atemperature of the urine measured with the temperature sensor 124.Furthermore, in one or more embodiments, the temperature sensor 124 maybe directly adjacent to the oxygen sensor 120. The foregoingconfiguration may increase accuracy of measurements. In one or moreembodiments, the temperature sensor 124 may include a thermistor. Forexample, the temperature sensor 124 may include a negative temperaturecoefficient (“NTC”) thermistor. For instance, the temperature sensor 124may include a temperature-sensing element including a semiconductormaterial that is sintered to display large changes in resistance inproportion to small changes in temperature. In further embodiments, thetemperature sensor 124 may be integrated with the flowrate sensor 122.

In some embodiments, the temperature sensor 124 may not be in contactwith the fluid (e.g., urine) flowing through the flow pathway 130 of theoxygen-sensing assembly 104. For example, the temperature sensor 124 mayinclude a non-contact sensor that compensates for material (e.g., awall) between the temperature sensor 124 and the fluid of which thetemperature sensor 124 is detecting temperature. For instance, thecontrol system 106 may adjust any detected temperature value tocompensate for a temperature loss across the material separating thetemperature sensor 124 and the fluid. Furthermore, the control system106 may utilize a temperature difference between what is measured withthe temperature sensor 124 and a temperature measured at a tip of theurinary catheter 102 to determine and compensate for temperature lossesor gains while flowing through the catheter assembly 100. In otherembodiments, the temperature sensor 124 may be positioned to come incontact with the fluid (e.g., urine) flowing through the flow pathway130 of the oxygen-sensing assembly 104. For instance, the temperaturesensor 124 may access the flow pathway 130 of the oxygen-sensingassembly 104 via a Tuohy-Borst clamp.

In further embodiments, the catheter assembly 100 may include a heatingelement and/or a cooling element for actively heat and/or cool urinepassing through flow pathway 130 of the oxygen-sensing assembly 104 andfor maintaining a temperature of the urine throughout at least a portionof the catheter assembly 100. In some embodiments, the catheter assembly100 may include at least one heating wire within the catheter assembly100 (e.g., within the flow pathway of the oxygen-sensing assembly 104)for heating the urine. In additional embodiments, the catheter assembly100 may include one or more thermoelectric coolers disposed within oraround portions of the catheter assembly for cooling the urine. Forinstance, the catheter assembly 100 may include one or more conventionalthermoelectric coolers. Maintaining a temperature of the urine with atleast a portion of the catheter assembly 100 may provide more consistentand accurate oxygen measurements, as described below.

Furthermore, the temperature sensor 124 may be operably coupled to thecontrol system 106 and may provide data related to a detectedtemperature of the fluid flowing through the flow pathway 130 of theoxygen-sensing assembly 104 to the control system 106. As is describedin greater detail in regard to FIG. 3, the control system 106 mayutilize the data related to the detected temperature of the fluid toadjust determined oxygen levels determined via the oxygen sensor 120.For instance, the control system 106 may adjust determined oxygen levelsbased on the detected temperature utilizing Henry's Law combined withVan′t Hoff's equation, as follows:

${Cond}_{{Dissolved}{Oxygen}} = {p_{o_{2}{Gas}} \times {k_{H}\left( {298.15K} \right)} \times e^{C_{O_{2}} \times {({\frac{1}{T} - \frac{1}{298.15K}})}}}$

Referring still to FIG. 1, the outlet end 128 of the oxygen-sensingassembly 104 may be attachable to a fluid collection container (e.g., aurine collection bag).

Additionally, in one or more embodiments, the oxygen-sensing assembly104 may include an additional oxygen sensor 140 (i.e., a second oxygensensor). The additional oxygen sensor 140 may extend through the balloonport 116 of the urinary catheter 102 and into the lumen 112 of theurinary catheter 102. Moreover, the additional oxygen sensor 140 mayinclude any of the oxygen sensor types described above in regard tooxygen sensor 120 (i.e., the first oxygen sensor). For instance, theadditional oxygen sensor 140 may include an optical fiber 142 and asensing portion 144. The sensing portion 144 of the additional oxygensensor 140 may be disposed within the lumen 112 of the urinary catheter102 in order to detect oxygen levels of a fluid (e.g., urine) in thebladder of the patient without extending out of the lumen 112 (e.g., theinlet end 108) of the urinary catheter 102. As a non-limiting example,the sensing portion 144 of the additional oxygen sensor 140 may besecured to the optical fiber 142 of the additional oxygen sensor 140, asdescribed above in regard to oxygen sensor 120. Furthermore, theadditional oxygen sensor 140 may operate and function via any of themanners described above in regard to oxygen sensor 120. Additionally,the additional oxygen sensor 140 may be operably coupled to the opticalmodule 136 of the control system 106. Because the oxygen-sensingassembly 104 includes two separate oxygen sensors, the control system106 may acquire two separate oxygen readings. As a result, theoxygen-sensing assembly 104 may provide more accurate oxygen readings incomparison to a single oxygen sensor.

One will appreciate that one or more computing device components may beemployed to implement the control system 106. The control system 106 mayinclude the optical module 136, a data acquisition system 146, aprocessor 148, a memory 150, a storage device 152, a user interface 154,and a communication interface 156, which may be communicatively coupledby way of a communication infrastructure 158. While one example of acomputing device is shown in FIG. 1, the components illustrated in FIG.1 are not intended to be limiting. Additional or alternative componentsmay be used in other embodiments. Furthermore, in certain embodiments,the control system 106 may include fewer components than those shown inFIG. 1. Components of the control system 106 shown in FIG. 1 aredescribed in additional detail below.

In one or more embodiments, the optical module 136 may provide (e.g.,generate) light (e.g., excitation beams) for the oxygen sensor 120 andadditional oxygen sensor 140. Furthermore, the optical module 136 mayreceive return light from the sensing portions 134, 144 of the oxygensensor 120 and the additional oxygen sensor 140. Moreover, the opticalmodule 136 may convert any received light into data and may provide thedata to the data acquisition system 146 of the control system 106. Asnoted above, in some embodiments, the optical module 136 may be disposedat and/or within the sensing portions 134, 144 of the oxygen sensor 120and the additional oxygen sensor 140 removing any need for an opticalfiber. As a non-limiting example, the optical module 136 may compriseany suitable optical module known in the art.

The data acquisition system 146 may receive signals from one or more ofthe optical module 136, temperature sensor 124, flowrate sensor 122,oxygen sensor 120, and/or additional oxygen sensor 140 and may include,or have associated therewith, analog to digital conversion circuitry toconvert the analog signals from the optical module and the varioussensors into digital numeric values that can be manipulated and/oranalyzed by the control system 106 (e.g., the processor 148 and/or thedata acquisition system 146 of the control system 106). The dataacquisition system 146 may further include one or more software programsdeveloped using various general purpose programming languages such asAssembly, BASIC, C, C++, C#, Fortran, Java, LabVIEW, Lisp, Pascal, etc.As a non-limiting example, the control system 106 may include any dataacquisition system known in the art.

In one or more embodiments, the processor 148 includes hardware forexecuting instructions, such as those making up a computer program. Asan example and not by way of limitation, to execute instructions, theprocessor 148 may retrieve (or fetch) the instructions from an internalregister, an internal cache, the memory 150, or the storage device 152and decode and execute them. In one or more embodiments, the processor148 may include one or more internal caches for data, instructions, oraddresses. As an example and not by way of limitation, the processor 148may include one or more instruction caches, one or more data caches, andone or more translation lookaside buffers (TLBs). Instructions in theinstruction caches may be copies of instructions in the memory 150 orthe storage 152.

As is described in greater detail in regard to FIGS. 2 and 3, thecontrol system 106 may utilize the optical module 136, data acquisitionsystem 146, and the processor 148 to determine urine oxygen tensionwithin the urine flowing through the flow pathway 130 of theoxygen-sensing assembly 104 based at least partially on one or more ofthe detected oxygen levels of the urine, the detected temperature of theurine, or the detected flowrate of the urine. Furthermore, based on thedetermined urine oxygen tension, the control system 106 may determine arisk of developing acute kidney injury (e.g., urinary hypoxia) in apatient. For instance, the control system 106 may diagnose kidneyhypoxia.

The memory 150 may be used for storing data, metadata, and programs forexecution by the processor(s). The memory 150 may include one or more ofvolatile and non-volatile memories, such as Random Access Memory(“RAM”), Read Only Memory (“ROM”), a solid state disk (“SSD”), Flash,Phase Change Memory (“PCM”), or other types of data storage. The memory150 may be internal or distributed memory.

The storage device 152 includes storage for storing data orinstructions. As an example and not by way of limitation, storage device152 can comprise a non-transitory storage medium described above. Thestorage device 152 may include a hard disk drive (HDD), a floppy diskdrive, flash memory, an optical disc, a magneto-optical disc, magnetictape, a Universal Serial Bus (USB) drive or a combination of two or moreof these. The storage device 152 may include removable or non-removable(or fixed) media, where appropriate. The storage device 152 may beinternal or external to the control system 106. In one or moreembodiments, the storage device 152 is non-volatile, solid-state memory.In other embodiments, the storage device 152 includes read-only memory(ROM). Where appropriate, this ROM may be mask programmed ROM,programmable ROM (PROM), erasable PROM (EPROM), electrically erasablePROM (EEPROM), electrically alterable ROM (EAROM), or flash memory or acombination of two or more of these.

The user interface 154 allows a user to provide input to, receive outputfrom, and otherwise transfer data to and receive data from controlsystem 106. The user interface 154 may include a mouse, a keypad or akeyboard, a touch screen, a camera, an optical scanner, networkinterface, modem, other known user devices or a combination of such userinterfaces. The user interface 154 may include one or more devices forpresenting output to a user, including, but not limited to, a graphicsengine, a display (e.g., a display screen), one or more output drivers(e.g., display drivers), one or more audio speakers, and one or moreaudio drivers. In certain embodiments, the user interface 154 isconfigured to provide graphical data to a display for presentation to auser. The graphical data may be representative of one or more graphicaluser interfaces and/or any other graphical content as may serve aparticular implementation.

The communication interface 156 may include hardware, software, or both.In any event, the communication interface 156 is configured to provideone or more interfaces for communication (such as, for example,packet-based communication) between the control system 106 and one ormore other computing devices or networks. As an example and not by wayof limitation, the communication interface 156 may include a networkinterface controller (NIC) or network adapter for communicating with anEthernet or other wire-based network or a wireless NIC (WNIC) orwireless adapter for communicating with a wireless network, such as aWI-FI.

Additionally or alternatively, the communication interface 156 mayfacilitate communications with an ad hoc network, a personal areanetwork (PAN), a local area network (LAN), a wide area network (WAN), ametropolitan area network (MAN), or one or more portions of the Internetor a combination of two or more of these. One or more portions of one ormore of these networks may be wired or wireless. As an example, thecommunication interface 156 may facilitate communications with awireless PAN (WPAN) (such as, for example, a BLUETOOTH WPAN), a WI-FInetwork, a WI-MAX network, a cellular telephone network (such as, forexample, a Global System for Mobile Communications (GSM) network), orother suitable wireless network or a combination thereof.

Additionally, the communication interface 156 may facilitatecommunications various communication protocols. Examples ofcommunication protocols that may be used include, but are not limitedto, data transmission media, communications devices, TransmissionControl Protocol (“TCP”), Internet Protocol (“IP”), File TransferProtocol (“FTP”), Telnet, Hypertext Transfer Protocol (“HTTP”),Hypertext Transfer Protocol Secure (“HTTPS”), Session InitiationProtocol (“SIP”), Simple Object Access Protocol (“SOAP”), ExtensibleMark-up Language (“XML”) and variations thereof, Simple Mail TransferProtocol (“SMTP”), Real-Time Transport Protocol (“RTP”), user DatagramProtocol (“UDP”), Global System for Mobile Communications (“GSM”)technologies, Code Division Multiple Access (“CDMA”) technologies, TimeDivision Multiple Access (“TDMA”) technologies, Short Message Service(“SMS”), Multimedia Message Service (“MMS”), radio frequency (“RF”)signaling technologies, Long Term Evolution (“LTE”) technologies,wireless communication technologies, in-band and out-of-band signalingtechnologies, and other suitable communications networks andtechnologies.

The communication infrastructure 158 may include hardware, software, orboth that couples components of the control system 106 to each other. Asan example and not by way of limitation, the communicationinfrastructure 158 may include an Accelerated Graphics Port (AGP) orother graphics bus, an Enhanced Industry Standard Architecture (EISA)bus, a front-side bus (FSB), a HYPERTRANSPORT (HT) interconnect, anIndustry Standard Architecture (ISA) bus, an INFINIBAND interconnect, alow-pin-count (LPC) bus, a memory bus, a Micro Channel Architecture(MCA) bus, a Peripheral Component Interconnect (PCI) bus, a PCI-Express(PCIe) bus, a serial advanced technology attachment (SATA) bus, a VideoElectronics Standards Association local (VLB) bus, or another suitablebus or a combination thereof.

Referring still to FIG. 1, in one or more embodiments, theoxygen-sensing assembly 104 may further include one or more valves(e.g., check valves) for directing fluid flow through the flow pathway130 of the oxygen-sensing assembly 104. As will be appreciated by one ofordinary skill in the art, including one or more valves for directingfluid flow through the flow pathway 130 of the oxygen-sensing assembly104 may prevent backflow and may reduce infection risks, and as aresult, may decrease sickness and disease that may be caused bycontamination and infection attributable to use of the disclosedembodiments. For instance, in embodiments where the of theoxygen-sensing assembly 104 includes a relatively larger lumen, a checkvalve may be useful to prevent pockets of air from moving up tubingextending to the fluid collection container and contaminating the oxygensensor 120 with oxygen. In embodiments utilizing a relatively smalllumen, the foregoing problem is eliminated as the lumen allows a surfacetension of the urine to prevent encroachment of bubbles.

FIG. 2 is a partial schematic representation of an oxygen sensor 220according to one or more embodiments of the present disclosure. Theoxygen sensor 220 of FIG. 2 may be utilized as either the oxygen sensor120 or the additional oxygen sensor 140 described in regard to FIG. 1.In some embodiments, the oxygen sensor 220 may include an optical fiber232 and a sensing portion 234. As described above, the optical fiber 232may include a core 260 and a cladding 262 and may be operable coupled tothe optical module 136 (FIG. 1) of the control system (FIG. 1).Additionally, the optical fiber 232 may transmit excitation light in afirst direction (e.g., toward a distal end of the optical fiber 232 andthe sensing portion 234) and return light in a second opposite direction(e.g., toward the optical module 136 of the control system 106 and fromthe sensing portion 234).

The sensing portion 234 may include a dye-impregnated polymer thatincludes and/or releases fluorescent dyes, which are excitable atselected wavelengths of light. For instance, the dye 264 may include oneor more of a platinum(II) based dye, a palladium(II) based dye, aruthenium(II) based dye, or a hemoglobin based dye. For example, the dye264 may include platinum octaethylporphyrin. Depending upon a partialpressure of oxygen molecules 266 (e.g., an amount of a quencher) withinthe urine flowing through flow pathway 130 of the oxygen-sensingassembly 104, a fluorescence (e.g., an amplitude and/or duration of afluorescence) of the dye 264 may vary. Furthermore, as described above,based on the fluorescence response (e.g., an amplitude and/or durationof the fluorescence response) of the dye 264, the control system 106 maydetermine oxygen levels within the urine.

In some embodiments, the sensing portion 234 may be disposed directly onthe distal end of the optical fiber 232. In alternative embodiments, thesensing portion 234 may be separate and distinct from the optical fiber232 (e.g., disposed away from the distal end of the optical fiber 232).Additionally, the sensing portion 234 may be sized, shaped, andconfigured to be disposed within the fluid flowing through the flowpathway 130 of the oxygen-sensing assembly 104. Furthermore, the oxygensensor 220 may operate via any of the manners described above in regardto FIG. 1.

FIG. 3 shows a method 300 that the control system 106 may utilize todetermine a risk of acute kidney injury (e.g., urinary hypoxia) in apatient. Referring to FIGS. 1-3 together, in some embodiments, themethod 300 may include generating an excitation light, as shown in act302 of FIG. 3. For example, the optical module 136 of the control system106 may generate the excitation light. In some embodiments, the opticalmodule 136 of the control system 106 may generate the excitation lightto have a selected wavelength of about 432 nm.

Additionally, the method 300 may include causing the excitation light tobe transmitted to a sensing portion 134 of an oxygen sensor 120, asshown in act 304 of FIG. 3. For example, the optical module 136 maytransmit the excitation light to the sensing portion 134 of the oxygensensor 120 through an optical fiber 132 of the oxygen sensor 120. Asdiscussed above, the sensing portion 134 of the oxygen sensor 120 may bedisposed within a fluid flowing through a flow pathway 130 of anoxygen-sensing assembly 104 of a catheter assembly 100.

In some embodiments, the method 300 may optionally include causing theexcitation light to be transmitted to an additional sensing portion 144of an additional oxygen sensor 140, as show in act 306 of FIG. 3. Asdiscussed above, the additional sensing portion 144 of the additionaloxygen sensor 140 may be disposed within a lumen 112 of a urinarycatheter 102 of the catheter assembly 100. The optical module 136 of thecontrol system 106 may transmit the excitation light to the additionalsensing portion 144 of the additional oxygen sensor 140 via any of themanners described above.

The method 300 may further include receiving return light from thesensing portion 134 of the oxygen sensor 120, as shown in act 308 ofFIG. 3. For example, as described above, the sensing portion 134 of theoxygen sensor 120 may include a dye-impregnated polymer that releasesfluorescent dyes 264, which are excitable at selected wavelengths oflight and may have a fluorescence response to the excitation light. Insome embodiments, the optical module 136 of the control system 106 mayreceive the return light from the sensing portion 134 via the opticalfiber 132.

Furthermore, the method 300 may optionally include receiving returnlight from the additional sensing portion 144 of the additional oxygensensor 140 of the oxygen-sensing assembly 104, as shown in act 310 ofFIG. 3. The optical module 136 of the control system 106 may receive thereturn light from the additional sensing portion 144 of the additionaloxygen sensor 140 via any of the manners described above in regard tothe sensing portion 134 of the oxygen sensor 120.

The method 300 may optionally include receiving temperature data andflowrate data from the temperature sensor 124 and the flowrate sensor122, as shown in act 312 of FIG. 3. For example, as discussed above, thetemperature sensor 124 and the flowrate sensor 122 may be operablycoupled to the control system 106 (e.g., the data acquisition system 146of the control system 106) and may provide data related to thetemperature and flowrate of a fluid (e.g., urine) flowing through theflow pathway 130 of the oxygen-sensing assembly 104.

Also, the method 300 may include comparing the return light receivedfrom the sensing portion 134 of the oxygen sensor 120 and/or theadditional sensing portion 144 of the additional oxygen sensor 140 tothe excitation light provided by the optical module 136, as shown in act314 of FIG. 3. For example, in some embodiments, the optical module 136of the control system 106 may provide a sinusoidally modulatedexcitation light, and the sensing portion 134 of the oxygen sensor 120and/or additional sensing portion 144 of the additional oxygen sensor140 may return a phase-shifted, sinusoidally modulated return light.Furthermore, the control system 106 may measure a phase shift of thephase-shifted, sinusoidally modulated return light relative to thesinusoidally modulated excitation light.

The method 300 may also include determining oxygen levels within thefluid flowing through the flow pathway 130 of the oxygen-sensingassembly 104 and/or the fluid flowing through the lumen 112 of theurinary catheter 102 of the catheter assembly 100, as shown in act 316of FIG. 3. For example, the control system 106 may determine oxygenlevels within the fluid based on the measured phase shift of thephase-shifted sinusoidally modulated return light relative to thesinusoidally modulated excitation light based on theStern-Vollmer-Theory described above in regard to FIG. 1. In someembodiments, determining oxygen levels may include determining dissolvedoxygen concentrations (mg/L), head space oxygen gas concentrations (%),dissolved oxygen readings, etc. In some embodiments, the control system106 may determine oxygen level within the fluid flowing through the flowpathway 130 of the oxygen-sensing assembly 104 and/or the fluid flowingthrough the lumen 112 of the urinary catheter 102 of the catheterassembly 100 in real-time based on measurements taken with the oxygensensor 120 and/or the additional oxygen sensor 140. In additionalembodiments, the control system 106 may further determine additionalmarkers such as, for example, pH, CO₂, bladder pressure, abdominalpressure, etc., utilizing the oxygen sensor 120, the additional oxygensensor 140, the temperature sensor 124, and/or the flowrate sensor 122.

In some embodiments, determining oxygen levels within the fluid flowingthrough the flow pathway 130 of the oxygen-sensing assembly 104 and/orthe fluid flowing through the lumen 112 of the urinary catheter 102 ofthe catheter assembly 100 may include adjusting the oxygen levels basedon a detected temperature and flowrate of the fluid. For instance, thecontrol system 106 may adjust determined oxygen levels based on thedetected temperature of the fluid utilizing Henry's Law combined withVan't Hoff's equation, as described above in regard to FIG. 1.Additionally, the control system 106 may adjust determined oxygen levelsbased on the detected flowrate of the fluid. For instance, the detectedflowrate may indicate how long the fluid has been out of the bladder ofthe patient. Accordingly, the control system 106 can adjust thedetermined oxygen levels based on how long the fluid has been out of thebladder and/or kidney of the patient and the fluid temperature, so thatthe determined oxygen levels reflect oxygen levels of the fluid withinthe bladder of the patient. For instance, the control system 106 mayutilize one or more algorithms having inputs of a volume of a urinecolumn between the renal medulla and the oxygen sensor 120, a diffusionof oxygen across kidney, ureter, bladder, urinary catheter, and/oroxygen-sensing assembly walls and membranes, flow rates of the urine,correlations between kidney PO2 and urine PO2, and body temperature toadjust the determined oxygen levels (e.g., output renal medulla PO2).Additionally, the control system 106 may plot determined oxygen levels(e.g., output renal medulla PO2) over time for a given patient.

Additionally, the method 300 may include determining oxygen tension ofthe fluid flowing through the flow pathway 130 of the oxygen-sensingassembly 104 and/or the fluid flowing through the lumen 112 of theurinary catheter 102 of the catheter assembly 100, as shown in act 318of FIG. 3. In some embodiments, the method 300 may include measuring theoxygen tension (pO2) (mmHg) (e.g., partial pressure) directly with theoxygen sensor 120. Additionally, the method 300 may include determiningurinary oxygen tension (pO2) (mmHg) and/or mean medullary oxygen tension(mmHg) based on the oxygen levels determined in act 316 of FIG. 3.

The method 300 may further include determining a risk of acute kidneyinjury (e.g., urinary hypoxia) of a patient based on the oxygentension(s) determined in act 318 of FIG. 3, as shown in act 320 of FIG.3. For example, the control system 106 may determine the risk ofdeveloping future acute kidney injury in the patient (e.g., kidneyhypoxia). Additionally, the control system 106 may cause an indicationof the risk of developing future acute kidney injury to be displayed onthe user interface 154 of the control system 106. Moreover, the method300 may include continuously repeating acts 302 through 320 tocontinuously monitor oxygen tension within the urine of the patient andto continuously monitor for risk of acute kidney injury in the patient.Furthermore, the control system 106 may cause an indication of aninstantaneous/real-time urine flow through the catheter assembly 100 tobe displayed on the user interface 154 of the control system 106.

In view of the foregoing, the catheter assembly 100 of the presentdisclosure may provide a continuous and real-time monitor of kidneyhypoxia for patients. Furthermore, because the catheter assembly 100monitors the urine of the patient in real-time, the catheter assembly100 may remove the inherent lag time present in conventional methods ofdiagnosing patients at risk of for a subsequent acute kidney injury(e.g., methods of measuring serum creatinine levels). As will beappreciated by one of ordinary skill in the art, by detecting kidneyhypoxia as indicated by urinary hypoxia, the catheter assembly 100 mayallow for detection of patients at risk for subsequent acute kidneyinjury. By identifying these patients at risk, before permanent kidneyinjury occurs, the catheter assembly 100 may prevent AKI, and thusreduce hospital stay durations, medical costs, improve recovery times,and may ultimately save lives.

Additionally, the catheter assembly 100 of the present disclosure mayprovide a relatively non-invasive method for continuously monitoring forkidney hypoxia and risk for acute kidney injury in patients. Forinstance, perioperative patients typically have a urinary catheterplaced before surgery, and use of the catheter assembly 100 of thepresent disclosure with urinary catheter 102 placed pre-operatively doesnot increase the invasiveness of the already placed catheter. Criticallyill non-operative patients also frequently have urinary catheters andare at significant risk for acute kidney injury. One advantage of thecatheter assembly 100 of the present disclosure is that the catheterassembly 100 may be introduced into any urinary catheter, even urinarycatheters that are already in place in the patient. As discussed above,all of the measurements (e.g., oxygen, temperature, and flowratemeasurements) take place within the catheter assembly 100. For instance,the oxygen-sensing assembly 104 may be placed after the urinary catheter102 is placed without requiring any more invasive procedures.Furthermore, the oxygen-sensing assembly 104 may give healthcareproviders more flexibility, as any decision regarding whether or not toinclude the oxygen-sensing assembly 104 need not be made prior tosurgery or hospital admission but can be made anytime throughout apatient's care without requiring additional invasive procedures.Accordingly, the catheter assembly 100 of the present disclosure mayreduce the risk of infection and disease by not increasing invasiveprocedures. Additionally, the catheter assembly 100 may be able usablewith a wide variety of different urinary catheters, and accordingly, mayprovide a more versatile catheter assembly to health care providers.Moreover, in comparison to conventional catheter assemblies, thecatheter assembly 100 of the present disclosure provides for simplerinstallation and less risk of infection, fiber breakage, and leaching offluorescent dyes into the body of the patient. Also, the catheterassembly 100 is connected to the control system 106 via reusable cables,making the oxygen-sensing assembly disposable and less expensive thanconventional fiber-up-catheter systems. Furthermore, the catheterassembly 100 may provide real-time urinary flowrates that may allowassessment of clinical interventions, such as vasoactive medications andadministration of fluids.

FIG. 4 shows a catheter assembly 400 according to one or moreembodiments of the present disclosure. As shown in FIG. 4, similar tothe catheter assembly 100 of FIG. 1, the catheter assembly 400 mayinclude a urinary catheter 402 and an oxygen-sensing assembly 404 influid communication with the urinary catheter 402. Additionally, thecatheter assembly 400 may be operably coupled to a control system 106 asshown and described above in regard to FIGS. 1-3. Additionally, theoxygen-sensing assembly 404 may include a housing 418, an oxygen sensor420, a flowrate sensor 422, and a temperature sensor 424. The oxygensensor 420, the flowrate sensor 422, and the temperature sensor 424 mayinclude any of the oxygen sensors, flowrate sensors, and temperaturesensors described above in regard to FIG. 1. The housing 418 may includean inlet end 426 and an outlet end 428 and may define a flow pathway 430between the inlet end 426 and the outlet end 428. The inlet end 426 ofthe housing 418 may be attachable to the outlet end 410 of the urinarycatheter 402 via any connection methods known in the art. The oxygensensor 420, the temperature sensor 424, and the flowrate sensor 422, maybe disposed along the flow pathway 430 in series.

The catheter assembly 400 may further include a check valve 470downstream of the oxygen sensor 420, the temperature sensor 424, and theflowrate sensor 422 along the flow pathway 430 of the oxygen-sensingassembly 404. Furthermore, in some embodiments, the catheter assembly400 may include a relief valve and pathway 472 that has a highercracking pressure (i.e., opening pressure) than the check valve suchthat flow of the fluid is biased through the check valve. In someembodiments, the relief valve and pathway 472 may extend from a locationalong the flow pathway 430 of the oxygen-sensing assembly 404 proximateto the temperature sensor 424 and may bypass the flowrate sensor 422. Asa result, the temperature sensor 424 and the oxygen sensor 420 cannot bebypassed via the relief valve and pathway 472. Additionally, the reliefvalve and pathway 472 provides a pathway for fluid flow in the event theflow pathway 430 of the oxygen-sensing assembly 404 becomes clogged orfails (e.g., a check valve within the flow pathway 430 of theoxygen-sensing assembly 404 becomes clogged or fails).

FIG. 5 shows a catheter assembly 500 according to one or moreembodiments of the present disclosure. As shown in FIG. 5, similar tothe catheter assembly 100 of FIG. 1, the catheter assembly 500 mayinclude a urinary catheter 502 and an oxygen-sensing assembly 504 influid communication with the urinary catheter 502. Additionally, thecatheter assembly 500 may be operably coupled to a control system 106 asshown and described above in regard to FIGS. 1-3. Additionally, theoxygen-sensing assembly 504 may include a housing 518, an oxygen sensor520, a flowrate sensor 522, and a temperature sensor 524. The oxygensensor 520, the flowrate sensor 522, and the temperature sensor 524 mayinclude any of the oxygen sensors, flowrate sensors, and temperaturesensors described above in regard to FIG. 1. The housing 518 may includean inlet end 526 and an outlet end 528 and may define a flow pathway 530between the inlet end 526 and the outlet end 528. The inlet end 526 ofthe housing 518 may be attachable to the outlet end 510 of the urinarycatheter 502 via any connection methods known in the art. The flowratesensor 522, the temperature sensor 524, and the oxygen sensor 520 may bedisposed along the flow pathway 530 in series.

The catheter assembly 500 may include three fluid pathways 560, 562, 564in parallel, each have a check valve, and each having a same crackingpressure (i.e., opening pressure). In additional embodiments, one ormore the check valves of the three fluid pathways 560, 562, 564 may havea higher cracking pressure. In some embodiments, the three fluidpathways 560, 562, 564 may be disposed after the flowrate sensor 522,the temperature sensor 524, and the oxygen sensor 520 along the flowpathway 530 of the oxygen-sensing assembly 504. Additionally, the threefluid pathways 560, 562, 564 provide pathways for fluid flow in theevent the flow pathway 530 of the oxygen-sensing assembly 504 becomesclogged or fails (e.g., a check valve within the flow pathway 530 of theoxygen-sensing assembly 504 becomes clogged or fails). Moreover, thethree fluid pathways 560, 562, 564 provide multiple safeguards in theevent one of the three fluid pathways 560, 562, 564 also fails.

Additional non limiting example embodiments of the disclosure aredescribed below.

Embodiment 1: A catheter assembly, comprising: a urinary cathetercomprising at least one lumen extending between an inlet end and anoutlet end; an oxygen-sensing assembly in fluid communication with theurinary catheter, the oxygen-sensing assembly comprising: a housinghaving flow pathway extending between an inlet end and an outlet endthereof, wherein the inlet end of the housing is attachable to theoutlet end of the urinary catheter; an oxygen sensor in operablecommunication with the flow pathway of the housing, the oxygen sensorconfigured to detect oxygen levels of a fluid flowing through the flowpathway; a flowrate sensor disposed between the oxygen sensor and theinlet end of the housing and configured to detect a flowrate of thefluid flowing through the flow pathway; and a temperature sensordisposed downstream of the oxygen sensor and configured to detect atemperature of the fluid flowing through the flow pathway; and a controlsystem operably coupled to the oxygen sensor, the flowrate sensor, andthe temperature sensor, the control system comprising: at least oneprocessor; and at least one non-transitory computer-readable storagemedium storing instructions thereon that, when executed by the at leastone processor, cause the control system to: receive a detected oxygenlevels, a detected flowrate, and a detected temperature of the fluidflowing through the flow pathway; and based at least partially on one ormore of the detected oxygen levels and the detected temperature,determine a measurement of an oxygen tension of the fluid flowingthrough the flow pathway of the housing.

Embodiment 2: The catheter assembly of embodiment 1, wherein the oxygensensor comprises a fiber-optic sensor.

Embodiment 3: The oxygen-sensing assembly of embodiment 1, wherein theoxygen sensor comprises a Fiber Bragg grating sensor.

Embodiment 4: The oxygen-sensing assembly of embodiment 1, wherein theoxygen sensor comprises an electrochemical sensor.

Embodiment 5: The catheter assembly of embodiment 1, wherein the oxygensensor comprises: an optical fiber extending at least partially into thehousing of the oxygen-sensing assembly; and a sensing portion disposedat least partially within the flow pathway of the housing and exposed tothe fluid flowing through the flow pathway of the housing, wherein theoptical fiber is configured to transmit light through a distal end ofthe optical fiber and toward the sensing portion and to receive lightfrom the sensing portion through the distal end of the optical fiber.

Embodiment 6: The catheter assembly of embodiment 5, wherein the controlsystem further comprises instructions that, when executed by the atleast one processor, cause the control system to: receive light throughthe optical fiber originating from the sensing portion of thefiber-optic sensor; analyze the light to determine a correlatingfluorescence; and based on the determined fluorescence, determine themeasurement of an oxygen tension of the fluid flowing through the flowpathway of the housing.

Embodiment 7: The catheter assembly of embodiments 2-6, wherein theoxygen sensor further comprises a barrier disposed between the opticalfiber and the sensing portion and configured to prevent the opticalfiber from coming into contact with the fluid flowing through the flowpathway of the housing.

Embodiment 8: The catheter assembly of embodiments 3-7, wherein thesensing portion comprises a dye-impregnated polymer that is excitable ata selected wavelength.

Embodiment 9: The catheter assembly of embodiments 1-8, wherein theoxygen-sensing assembly further comprises an additional oxygen sensordisposed within the at least one lumen of the urinary catheter and at atip of the at least one lumen.

Embodiment 10: The catheter assembly of embodiment 9, wherein theadditional oxygen sensor comprises: an additional optical fiberextending into the at least one lumen of the catheter; and an additionalsensing portion disposed on a distal end of the optical fiber within thelumen of the catheter, wherein the additional optical fiber isconfigured to transmit light through a distal end of the additionaloptical fiber and toward the additional sensing portion and to receivelight from the additional sensing portion through the distal end of theadditional optical fiber.

Embodiment 11: An oxygen-sensing assembly for attachment to a urinarycatheter, the oxygen-sensing assembly comprising: a housing having aflow pathway extending between an inlet end and an outlet end thereof;and an oxygen sensor in operable communication with the flow pathway ofthe housing, the oxygen sensor configured to detect oxygen levels of afluid flowing through the flow pathway.

Embodiment 12: The oxygen-sensing assembly of embodiment 11, wherein theoxygen sensor comprises a fiber-optic sensor.

Embodiment 13: The oxygen-sensing assembly of embodiments 11 and 12,wherein the oxygen sensor comprises a Fiber Bragg grating sensor.

Embodiment 14: The oxygen-sensing assembly of embodiment 11, furthercomprising: a flowrate sensor disposed between the oxygen sensor and theinlet end of the housing and configured to detect a flowrate of thefluid flowing through the flow pathway; and a temperature sensordisposed downstream of the oxygen sensor and configured to detect atemperature of the fluid flowing through the flow pathway.

Embodiment 15: The oxygen-sensing assembly of embodiment 11, wherein theoxygen sensor comprises: an optical fiber extending at least partiallyinto the housing of the oxygen-sensing assembly; and a sensing portiondisposed at least partially within the flow pathway of the housing andexposed to the fluid flowing through the flow pathway of the housing,wherein the optical fiber is configured to transmit light through adistal end of the optical fiber and at the sensing portion and toreceive light from the sensing portion through the distal end of theoptical fiber.

Embodiment 16: The catheter assembly of embodiment 15, wherein thesensing portion comprises a dye-impregnated polymer that is excitable ata selected wavelength.

Embodiment 17: The oxygen-sensing assembly of embodiments 11-16, furthercomprising a one-way valve disposed within the housing downstream fromthe oxygen sensor along the flow pathway.

Embodiment 18: The catheter assembly of embodiments 11-17, wherein theoxygen-sensing assembly further comprises additional oxygen sensordisposable within a lumen of the urinary catheter.

Embodiment 19: The oxygen-sensing assembly of embodiment 11, furthercomprising at least one relief valve oriented parallel to at least aportion of the flow pathway.

Embodiment 20: A method, comprising: attaching an oxygen-sensingassembly to a urinary catheter; disposing the urinary catheter within abladder of a subject; detecting oxygen levels of a fluid flowing throughthe urinary catheter and through a flow pathway of a housing of theoxygen-sensing assembly with an oxygen sensor; detecting a flowrate ofthe fluid flowing through the flow pathway with a flowrate sensor;detecting a temperature of the fluid flowing through the flow pathwaywith a temperature sensor; and based at least partially on one or moreof the detected oxygen levels and the detected temperature of the fluid,determining a measurement of an oxygen tension of the fluid flowingthrough the flow pathway.

Embodiment 21: The method of embodiment 20, further comprisingpositioning an additional oxygen sensor within a lumen of the urinarycatheter.

Embodiment 22: The method of embodiments 20 and 21, wherein detecting alevel of oxygen tension of a fluid further comprises: transmitting lightat a selected wavelength through an optical fiber of the oxygen sensorand toward a sensing portion of the oxygen sensor disposed within theflow pathway; receiving light through the optical fiber of the oxygensensor emitted from the sensing portion of the oxygen sensor; analyzingthe received light to determine a correlating fluorescence; anddetermining a urinary oxygen tension based on the determinefluorescence.

Embodiment 23: The method of embodiments 20-22, further comprisingdetermining from the determined measurement of the oxygen tension of thefluid flowing through the flow pathway if urinary hypoxia is indicated.

Embodiment 24: The method of embodiment 20, further comprisingcalculating via one or more algorithms a medullary pO2.

Embodiment 25: The method of embodiment 20, further comprisingdisplaying a real-time urine flowrate on a user interface of a controlsystem.

While the present invention has been described herein with respect tocertain illustrated embodiments, those of ordinary skill in the art willrecognize and appreciate that it is not so limited. Rather, manyadditions, deletions, and modifications to the illustrated embodimentsmay be made without departing from the scope of the invention asclaimed, including legal equivalents thereof. In addition, features fromone embodiment may be combined with features of another embodiment whilestill being encompassed within the scope of the invention ascontemplated by the inventors. Further, embodiments of the disclosurehave utility with different and various tool types and configurations.

1. An assembly comprising an oxygen-sensing assembly, the oxygen-sensingassembly comprising: a housing having a flow pathway extending betweenan inlet end and an outlet end thereof, the inlet end configured to beattachable to a device transmitting bodily fluids from a patient; and anoxygen sensor in operable communication with the flow pathway of thehousing, the oxygen sensor configured to detect oxygen levels of a fluidflowing through the flow pathway.
 2. The assembly of claim 1, whereinthe oxygen sensor comprises a fiber-optic sensor.
 3. (canceled)
 4. Theassembly of claim 1, further comprising at least one of: a flowratesensor configured to detect a flowrate of the fluid flowing through theflow pathway; and a temperature sensor configured to detect atemperature of the fluid flowing through the flow pathway.
 5. Theassembly of claim 2, wherein the oxygen sensor comprises: an opticalfiber extending at least partially into the housing of theoxygen-sensing assembly; and a sensing portion disposed at leastpartially within the flow pathway and exposed to the fluid flowingthrough the flow pathway, wherein the optical fiber is configured toemit light through a distal end of the optical fiber to the sensingportion and to receive light from the sensing portion through the distalend of the optical fiber.
 6. The assembly of claim 5, wherein thesensing portion comprises a dye-impregnated material that is excitableat a selected wavelength. 7-9. (canceled)
 10. The assembly of claim 1,wherein the inlet end of the housing is configured to be attached to acatheter.
 11. The assembly of claim 5, further comprising a controlsystem operably coupled to the optical fiber, the control systemcomprising at least one non-transitory computer-readable storage mediumstoring instructions thereon that, when executed by at least oneprocessor, cause the control system to: receive the received light fromthe sensing portion through the optical fiber; analyze the light todetermine a fluorescence; and based on the determined fluorescence,determine a measurement of oxygen tension of the fluid flowing throughthe flow pathway.
 12. The assembly of claim 5, further comprising abarrier member between the sensing portion and the optical fiber toprevent contact between the optical fiber and the fluid flowing throughthe flow pathway.
 13. The assembly of claim 1, wherein the oxygen sensorcomprises an electrochemical sensor.
 14. The assembly of claim 1,wherein the oxygen sensor comprises: an excitation portion configured togenerate light; a sensing portion configured to receive the generatedlight from the excitation portion; and an optical module that receivesthe light from the sensing portion.
 15. The assembly of claim 14,further comprising a control system operably coupled to the sensingportion, the control system comprising at least one non-transitorycomputer-readable storage medium storing instructions thereon that, whenexecuted by at least one processor, cause the control system to: receivethe light from the sensing portion; analyze the light to determine afluorescence; and based on the determined fluorescence, determine ameasurement of oxygen tension of the fluid flowing through the flowpathway.
 16. The assembly of claim 15 further comprising a barriermember between the sensing portion and the excitation portion to preventcontact between the excitation portion and the fluid flowing through theflow pathway.
 17. The assembly of claim 15, wherein the sensing portioncomprises a dye-impregnated material exhibiting a fluorescence based onan oxygen tension of a fluid to which it is exposed.
 18. The assembly ofclaim 1, further comprising a control system configured to determine adifference in a temperature of the fluid in a patient and a temperatureof the fluid in the flow pathway.
 19. The assembly of claim 4, furthercomprising a control system operably coupled to the oxygen sensor, thecontrol system comprising at least one non-transitory computer-readablestorage medium storing instructions thereon that, when executed by atleast one processor, cause the control system to: based at leastpartially on at least one of the detected oxygen level, the detectedflowrate, and the detected temperature, qualify the at least onedetected oxygen level to determine a relevance of the at least onedetected oxygen level to one or more of a bladder oxygen tension, akidney oxygen tension, and an oxygen level of the fluid in the flowpathway.
 20. The assembly of claim 4, further comprising a controlsystem operably coupled to the oxygen sensor, the control systemcomprising at least one non-transitory computer-readable storage mediumstoring instructions thereon that, when executed by at least oneprocessor, cause the control system to: based at least partially on atleast one of the detected oxygen level, the detected flowrate, and thedetected temperature, determine an oxygen level of the fluid in abladder or a kidney of a patient.
 21. The assembly of claim 20, whereinthe control system is configured to, based at least partially on theoxygen level of the fluid in the bladder or the kidney of the patient,at least one of determine a risk of acute kidney injury of the patientand diagnose kidney hypoxia.
 22. The assembly of claim 1, furthercomprising a control system in operable communication with theoxygen-sensing assembly, the control system comprising: an opticalmodule coupled to the oxygen-sensing assembly; and a communicationinterface coupled to the optical module.
 23. The assembly of claim 1,further comprising a control system in operable communication with theoxygen sensor, the control system comprising at least one non-transitorycomputer-readable storage medium storing instructions thereon that, whenexecuted by at least one processor, cause the control system to: basedat least partially on at least one of a detected oxygen level of thefluid in the flow pathway, a detected flowrate of the fluid in the flowpathway, and a detected temperature of the fluid in the flow pathway,determine an oxygen level of the fluid in a bladder or a kidney of apatient.
 24. The assembly of claim 1, further comprising a controlsystem in operable communication with the oxygen sensor, the controlsystem comprising at least one non-transitory computer-readable storagemedium storing instructions thereon that, when executed by at least oneprocessor, cause the control system to: based at least partially on atleast one of a detected oxygen level of the fluid in the flow pathway, adetected flowrate of the fluid in the flow pathway, data from a flowratesensor, and a detected temperature of the fluid in the flow pathway,qualify the at least one detected oxygen level to determine a relevanceof the at least one detected oxygen level to one or more of a bladderoxygen tension, a kidney oxygen tension, and an oxygen level of thefluid in the flow pathway.